OPTICALLY PURE AND FLUORO SUBSTITUTED CARBOACYCLIC NUCLEOSIDE ANALOGS

被引：13

作者：

BRAVO, P

FRIGERIO, M

SOLOSHONOK, V

VIANI, F

机构：

[1] CNR - Centro, Studio per le Sostanze Organiche Naturali - Dipartimento di Chimica, Politecnico di Milano, I-20131 Milano

来源：

TETRAHEDRON LETTERS | 1993年 / 34卷 / 48期

关键词：

D O I：

10.1016/S0040-4039(00)61562-9

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

Fluorinated analogues of carboacyclic nucleosides are obtained in optically pure form starting from homochiral epoxides through nitrogen nucleophilic opening of the oxirane ring.

引用

页码：7771 / 7772

页数：2

共 5 条

[1] NUCLEOCYCLITOLS - SYNTHESIS OF SUBSTITUTED PURINYL-MUCO-INOSITOL DERIVATIVES
AGUILAR, GJ
GELPI, ME
CADENAS, RA
[J]. JOURNAL OF HETEROCYCLIC CHEMISTRY, 1992, 29 (02) : 401 - 405
[2] A NEW VERSATILE FLUORINATED-C(4) CHIRON
ARNONE, A
BRAVO, P
CAVICCHIO, G
FRIGERIO, M
MARCHETTI, V
VIANI, F
ZAPPALA, C
[J]. TETRAHEDRON LETTERS, 1992, 33 (38) : 5609 - 5612
[3] GENERAL-SYNTHESIS OF CARBANUCLEOSIDES VIA REGIOSPECIFIC EPOXIDE OPENING BY THE AGLYCONE
BAUMGARTNER, H
MARSCHNER, C
PUCHER, R
GRIENGL, H
[J]. TETRAHEDRON LETTERS, 1991, 32 (05) : 611 - 614
[4] OPTICALLY PURE AND FLUOROSUBSTITUTED ACYCLOVIR ANALOGS
BRAVO, P
RESNATI, G
VIANI, F
[J]. TETRAHEDRON, 1993, 49 (03) : 713 - 720
[5] SYNTHESIS OF HYDROXYLATED CYCLOHEXENYLADENINES AND CYCLOHEXANYLADENINES AS POTENTIAL INHIBITORS OF S-ADENOSYLHOMOCYSTEINE HYDROLASE
RAMESH, K
WOLFE, MS
LEE, Y
VELDE, DV
BORCHARDT, RT
[J]. JOURNAL OF ORGANIC CHEMISTRY, 1992, 57 (22) : 5861 - 5868

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